Canonical Allele Identifier: CA6681067
Gene: LRRC10 HGNC NCBI
MyVariant.info:
GRCh38 chr12:g.69610386G>A
GRCh37 chr12:g.70004166G>A
gnomAD v2:
12:70004166 G / A
gnomAD v3:
12:69610386 G / A
gnomAD v4:
chr12-69610386-G-A
Joint Max Group AF 0.03273942 (EAS)
Genomes Max Group AF 0.02268184 (EAS)
Exomes Max Group AF 0.03365633 (EAS)
ClinVar Allele:
527880
ClinVar RCV:
RCV000655489
RCV001775943
ClinVar Variation:
544368
dbSNP:
12229290
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69610386G>A , CM000674.2:g.69610386G>A GRCh38
NC_000012.11:g.70004166G>A , CM000674.1:g.70004166G>A GRCh37
NC_000012.10:g.68290433G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361484.5:c.453C>T MANE Select ENSP00000355166.3:p.Ala151=
ENST00000361484.4:c.453C>T ENSP00000355166.3:p.Ala151=
NM_201550.3:c.453C>T NP_963844.2:p.Ala151=
NM_201550.4:c.453C>T MANE Select NP_963844.2:p.Ala151=
Search 100 bp 5'
Search 100 bp 3'